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FDA Import Refusal 799-7198510-5/11/1 — Abbott Rapid Diagnostics Jena GmbH

Abbott Rapid Diagnostics Jena GmbH — FEI 3016704892

The FDA refused shipment 799-7198510-5/11/1 from Abbott Rapid Diagnostics Jena GmbH (Germany) on Feb 2, 2022. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charges: 237,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Feb 2, 2022
Country
Germany
Product Category
Devices
Product Code
83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
Charges
237,508

Other import refusals

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.